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| Plasmid Name | Proper Citation | Insert Name | Organism | Bacterial Resistance | Defining Citation |
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Magoh198delG Resource Report Resource Website |
RRID:Addgene_30481 | Magoh | Mus musculus | Ampicillin | PMID:20364144 | AluI digestion generates 341 bp, 189 bp, 112 bp. Wt only generates 341 bp +300 bp fragments. | Backbone Marker:Invitrogen; Backbone Size:4400; Vector Backbone:pCMV-Sport6; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | 198delG (point nucleotide deletion) | Addgene | 2026-11-07 01:13:42 | 0 |
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pcDNA-HDAC6.ΔBuz-FLAG Resource Report Resource Website 1+ mentions |
RRID:Addgene_30484 | HDAC6 | Homo sapiens | Ampicillin | PMID:14675537 | Backbone Marker:Invitrogen; Backbone Size:5400; Vector Backbone:pcDNA3; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | Deletion of the C-terminal Ubiquitin binding domain- aa1044-1273 (BUZ domain) | Addgene | 2026-11-07 01:13:42 | 3 | |
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pcDNA-HDAC6.DC-FLAG Resource Report Resource Website 10+ mentions |
RRID:Addgene_30483 | HDAC6 | Homo sapiens | Ampicillin | PMID:14675537 | Backbone Marker:Invitrogen; Backbone Size:5400; Vector Backbone:pcDNA3; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | Catalytically inactive mutant (H216/611A) | Addgene | 2026-11-07 01:13:42 | 12 | |
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pcDNA-HDAC4.3SA-FLAG Resource Report Resource Website 1+ mentions |
RRID:Addgene_30486 | HDAC4 | Homo sapiens | Ampicillin | Backbone Marker:Invitrogen; Backbone Size:5400; Vector Backbone:pcDNA3; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | S246/467/632A | Addgene | 2026-11-07 01:13:42 | 6 | ||
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pLV.SP146.gp91.GP91.cHS4 Resource Report Resource Website 1+ mentions |
RRID:Addgene_30480 | SP146/gp91/GP91/cHS4 | Ampicillin | PMID:21544095 | From the paper (note that some of these features may not be in this plasmid): All vectors were based on the pRRL-cPPT-hPGK-mcs-WPRE vector, derived from the pRRL-cPPT-hPGKeGFP-WPRE construct. The gp91promoter is the natural myeloid-specific promoter. The CMVenh comes from the peGFP-N1(Clontech, Saint-Germain-en-Laye, France), the synthetic intron from the pMG5 and the EF1a intron from the pWPI vector http://www.addgene.org/12254 The myeloid-specific enhancer SP107 and SP146 were provided by Senlin Li (Department of Medicine, UTHSCSA, San Antonio, TX, USA). The cHS4 insulator corresponds to the chicken beta-globin 5’-DNase I-hypersensitive site and was provided by Patrick Salmon (Department of Neuroscience, Faculty of Medicine, University of Geneva, Switzerland). | Backbone Size:0; Vector Backbone:pLV; Vector Types:Lentiviral; Bacterial Resistance:Ampicillin | Addgene | 2026-11-07 01:13:42 | 3 | ||
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pCMVβ-p300-myc Resource Report Resource Website 10+ mentions |
RRID:Addgene_30489 | p300 | Homo sapiens | Ampicillin | Backbone Size:4800; Vector Backbone:pCMVb; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | Addgene | 2026-11-07 01:13:42 | 25 | |||
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pCSHSP:Cre Resource Report Resource Website |
RRID:Addgene_30524 | Cre recombinase | bacteriophage P1 | Ampicillin | PMID:19266305 | Cre driven by Xenopus laevis heat shock 70 (hsp70) promoter Please note that there are some small discrepancies between Addgene's quality control sequence and the assembled sequence from the depositor. These discrepancies should not affect the function of the plasmid. | Backbone Size:3000; Vector Backbone:pCSGFP2; Vector Types:Mammalian Expression, Cre/Lox, heat shock inducible; Bacterial Resistance:Ampicillin | Addgene | 2026-11-07 01:13:42 | 0 | |
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pLV.CMVenh.gp91.eGFP.cHS4 Resource Report Resource Website |
RRID:Addgene_30471 | CMVenh/gp91/eGFP/cHS4 | Ampicillin | PMID:21544095 | From the paper (note that some of these features may not be in this plasmid): All vectors were based on the pRRL-cPPT-hPGK-mcs-WPRE vector, derived from the pRRL-cPPT-hPGKeGFP-WPRE construct. The gp91promoter is the natural myeloid-specific promoter. The CMVenh comes from the peGFP-N1(Clontech, Saint-Germain-en-Laye, France), the synthetic intron from the pMG5 and the EF1a intron from the pWPI vector http://www.addgene.org/12254 The myeloid-specific enhancer SP107 and SP146 were provided by Senlin Li (Department of Medicine, UTHSCSA, San Antonio, TX, USA). The cHS4 insulator corresponds to the chicken beta-globin 5’-DNase I-hypersensitive site and was provided by Patrick Salmon (Department of Neuroscience, Faculty of Medicine, University of Geneva, Switzerland). | Backbone Size:0; Vector Backbone:pLV; Vector Types:Lentiviral; Bacterial Resistance:Ampicillin | Addgene | 2026-11-07 01:13:42 | 0 | ||
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pRRL.SP107.gp91.eGFP Resource Report Resource Website |
RRID:Addgene_30473 | SP107/gp91/eGFP | Ampicillin | PMID:21544095 | From the paper (note that some of these features may not be in this plasmid): All vectors were based on the pRRL-cPPT-hPGK-mcs-WPRE vector, derived from the pRRL-cPPT-hPGKeGFP-WPRE construct. The gp91promoter is the natural myeloid-specific promoter. The CMVenh comes from the peGFP-N1(Clontech, Saint-Germain-en-Laye, France), the synthetic intron from the pMG5 and the EF1a intron from the pWPI vector http://www.addgene.org/12254 The myeloid-specific enhancer SP107 and SP146 were provided by Senlin Li (Department of Medicine, UTHSCSA, San Antonio, TX, USA). The cHS4 insulator corresponds to the chicken beta-globin 5’-DNase I-hypersensitive site and was provided by Patrick Salmon (Department of Neuroscience, Faculty of Medicine, University of Geneva, Switzerland). | Backbone Size:6800; Vector Backbone:pRRL; Vector Types:Lentiviral; Bacterial Resistance:Ampicillin | Addgene | 2026-11-07 01:13:42 | 0 | ||
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pRRL.SP146.gp47.eGFP Resource Report Resource Website |
RRID:Addgene_30475 | SP146/gp47 | Ampicillin | PMID:21544095 | From the paper (note that some of these features may not be in this plasmid): All vectors were based on the pRRL-cPPT-hPGK-mcs-WPRE vector, derived from the pRRL-cPPT-hPGKeGFP-WPRE construct. The gp91promoter is the natural myeloid-specific promoter. The CMVenh comes from the peGFP-N1(Clontech, Saint-Germain-en-Laye, France), the synthetic intron from the pMG5 and the EF1a intron from the pWPI vector http://www.addgene.org/12254 The myeloid-specific enhancer SP107 and SP146 were provided by Senlin Li (Department of Medicine, UTHSCSA, San Antonio, TX, USA). The cHS4 insulator corresponds to the chicken beta-globin 5’-DNase I-hypersensitive site and was provided by Patrick Salmon (Department of Neuroscience, Faculty of Medicine, University of Geneva, Switzerland). | Backbone Size:6800; Vector Backbone:pRRL; Vector Types:Lentiviral; Bacterial Resistance:Ampicillin | Addgene | 2026-11-07 01:13:42 | 0 | ||
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pRRL.SP146.gp91.eGFP Resource Report Resource Website |
RRID:Addgene_30474 | SP146/gp91/eGFP | Ampicillin | PMID:21544095 | From the paper (note that some of these features may not be in this plasmid): All vectors were based on the pRRL-cPPT-hPGK-mcs-WPRE vector, derived from the pRRL-cPPT-hPGKeGFP-WPRE construct. The gp91promoter is the natural myeloid-specific promoter. The CMVenh comes from the peGFP-N1(Clontech, Saint-Germain-en-Laye, France), the synthetic intron from the pMG5 and the EF1a intron from the pWPI vector http://www.addgene.org/12254 The myeloid-specific enhancer SP107 and SP146 were provided by Senlin Li (Department of Medicine, UTHSCSA, San Antonio, TX, USA). The cHS4 insulator corresponds to the chicken beta-globin 5’-DNase I-hypersensitive site and was provided by Patrick Salmon (Department of Neuroscience, Faculty of Medicine, University of Geneva, Switzerland). | Backbone Size:6800; Vector Backbone:pRRL; Vector Types:Lentiviral; Bacterial Resistance:Ampicillin | Addgene | 2026-11-07 01:13:42 | 0 | ||
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pLV.SP146.gp91.eGFP.cHS4 Resource Report Resource Website |
RRID:Addgene_30476 | SP146/gp91/eGFP/cHS4 | Ampicillin | PMID:21544095 | From the paper (note that some of these features may not be in this plasmid): All vectors were based on the pRRL-cPPT-hPGK-mcs-WPRE vector, derived from the pRRL-cPPT-hPGKeGFP-WPRE construct. The gp91promoter is the natural myeloid-specific promoter. The CMVenh comes from the peGFP-N1(Clontech, Saint-Germain-en-Laye, France), the synthetic intron from the pMG5 and the EF1a intron from the pWPI vector http://www.addgene.org/12254 The myeloid-specific enhancer SP107 and SP146 were provided by Senlin Li (Department of Medicine, UTHSCSA, San Antonio, TX, USA). The cHS4 insulator corresponds to the chicken beta-globin 5’-DNase I-hypersensitive site and was provided by Patrick Salmon (Department of Neuroscience, Faculty of Medicine, University of Geneva, Switzerland). | Backbone Size:0; Vector Backbone:pLV; Vector Types:Lentiviral; Bacterial Resistance:Ampicillin | Addgene | 2026-11-07 01:13:42 | 0 | ||
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pRRL.CMVenh.gp91.GP91 Resource Report Resource Website |
RRID:Addgene_30478 | CMVenh/gp91/GP91 | Ampicillin | PMID:21544095 | From the paper (note that some of these features may not be in this plasmid): All vectors were based on the pRRL-cPPT-hPGK-mcs-WPRE vector, derived from the pRRL-cPPT-hPGKeGFP-WPRE construct. The gp91promoter is the natural myeloid-specific promoter. The CMVenh comes from the peGFP-N1(Clontech, Saint-Germain-en-Laye, France), the synthetic intron from the pMG5 and the EF1a intron from the pWPI vector http://www.addgene.org/12254 The myeloid-specific enhancer SP107 and SP146 were provided by Senlin Li (Department of Medicine, UTHSCSA, San Antonio, TX, USA). The cHS4 insulator corresponds to the chicken beta-globin 5’-DNase I-hypersensitive site and was provided by Patrick Salmon (Department of Neuroscience, Faculty of Medicine, University of Geneva, Switzerland). | Backbone Size:6800; Vector Backbone:pRRL; Vector Types:Lentiviral; Bacterial Resistance:Ampicillin | Addgene | 2026-11-07 01:13:42 | 0 | ||
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pCS2+ Bmi1-cherry-HA Resource Report Resource Website |
RRID:Addgene_30516 | Bmi1 | Mus musculus | Ampicillin | PMID:21552206 | Backbone Size:4918; Vector Backbone:pCS2+ att-cherry-HA (C-term cherry-HA); Vector Types:Mammalian Expression, Xenopus/Zebrafish expression; Bacterial Resistance:Ampicillin | NO STOP | Addgene | 2026-11-07 01:13:42 | 0 | |
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pCS2+ macroH2A1.2-GFP-HA Resource Report Resource Website 1+ mentions |
RRID:Addgene_30515 | macroH2A1.2-C | Mus musculus | Ampicillin | PMID:21552206 | Vector Backbone:pDEST pCS2+ att-eGFP-HA (C term eGFP-HA); Vector Types:Mammalian Expression, Xenopus/Zebrafish expression.; Bacterial Resistance:Ampicillin | NO STOP | Addgene | 2026-11-07 01:13:42 | 2 | |
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pSUPER retro puro macroH2A2 shRNA Resource Report Resource Website |
RRID:Addgene_30518 | mH2A2 shRNA | Mus musculus | Ampicillin | PMID:21552206 | mH2A2 shRNA: 5’-GCAGAGGACAAGAAGCTTAAA | Backbone Marker:OligoEngine; Backbone Size:6343; Vector Backbone:pSUPER retro puro; Vector Types:Mammalian Expression, Retroviral, RNAi; Bacterial Resistance:Ampicillin | Addgene | 2026-11-07 01:13:42 | 0 | |
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pSUPER retro puro macroH2A1 shRNA Resource Report Resource Website |
RRID:Addgene_30517 | mH2A1 shRNA | Mus musculus | Ampicillin | PMID:21552206 | H2A1 shRNA: 5’-GGGTGCAGACAAATGTGAA | Backbone Marker:OligoEngine; Backbone Size:6343; Vector Backbone:pSUPER retro puro; Vector Types:Mammalian Expression, Retroviral, RNAi; Bacterial Resistance:Ampicillin | Addgene | 2026-11-07 01:13:42 | 0 | |
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(-6kb/-207)-GFP Resource Report Resource Website |
RRID:Addgene_30462 | HNF1a promoter | Xenopus laevis | Ampicillin | PMID:10585563 | The GFP variant in the plasmid backbone, pCSGFP2, contains the F64L and the S65T mutations resulting in 35 times brighter green emission (as described in Ikawa M et al., Curr. Top. Dev. Biol. 44 (1999), pp. 1–20) This construct is derived from the (−6 kb/−58)-GFP construct [Addgene plasmid number 30460] by replacing the EcoRI–HindIII fragment (−494 to −58) with the corresponding EcoRI–HindIII fragment (−494 to −207) of the 3Δ207 clone (as described in Zapp D et al., Mol. Cell. Biol. 13 (1993), pp. 6416–6426). | Backbone Size:3812; Vector Backbone:pCSGFP2; Vector Types:Mammalian Expression; Bacterial Resistance:Ampicillin | Addgene | 2026-11-07 01:13:41 | 0 | |
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pRRL.gp91.EF1aIntron.eGFP Resource Report Resource Website |
RRID:Addgene_30466 | CMVenh/gp91/EF1aIntron/eGFP | Ampicillin | PMID:21544095 | From the paper (note that some of these features may not be in this plasmid): All vectors were based on the pRRL-cPPT-hPGK-mcs-WPRE vector, derived from the pRRL-cPPT-hPGKeGFP-WPRE construct. The gp91promoter is the natural myeloid-specific promoter. The CMVenh comes from the peGFP-N1(Clontech, Saint-Germain-en-Laye, France), the synthetic intron from the pMG5 and the EF1a intron from the pWPI vector http://www.addgene.org/12254 The myeloid-specific enhancer SP107 and SP146 were provided by Senlin Li (Department of Medicine, UTHSCSA, San Antonio, TX, USA). The cHS4 insulator corresponds to the chicken beta-globin 5’-DNase I-hypersensitive site and was provided by Patrick Salmon (Department of Neuroscience, Faculty of Medicine, University of Geneva, Switzerland). | Backbone Size:6800; Vector Backbone:pRRL; Vector Types:Lentiviral; Bacterial Resistance:Ampicillin | Addgene | 2026-11-07 01:13:41 | 0 | ||
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pRRL.CMVenh.gp91.eGFP Resource Report Resource Website |
RRID:Addgene_30468 | CMVenh/gp91/EGFP | Ampicillin | PMID:21544095 | From the paper (note that some of these features may not be in this plasmid): All vectors were based on the pRRL-cPPT-hPGK-mcs-WPRE vector, derived from the pRRL-cPPT-hPGKeGFP-WPRE construct. The gp91promoter is the natural myeloid-specific promoter. The CMVenh comes from the peGFP-N1(Clontech, Saint-Germain-en-Laye, France), the synthetic intron from the pMG5 and the EF1a intron from the pWPI vector http://www.addgene.org/12254 The myeloid-specific enhancer SP107 and SP146 were provided by Senlin Li (Department of Medicine, UTHSCSA, San Antonio, TX, USA). The cHS4 insulator corresponds to the chicken beta-globin 5’-DNase I-hypersensitive site and was provided by Patrick Salmon (Department of Neuroscience, Faculty of Medicine, University of Geneva, Switzerland). | Backbone Size:6800; Vector Backbone:pRRL; Vector Types:Lentiviral; Bacterial Resistance:Ampicillin | Addgene | 2026-11-07 01:13:42 | 0 |
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